Asperphenamate 产品活性：Asperphenamate 是来自Aspergillus flatiipes 的真菌代谢物，具有抗肿瘤活性，其对 T47D、MDA-MB-231 和 HL-60 细胞的IC50 值分别为 92.3 μM、96.5 μM 和97.9 μM。 产品来源： https://www.medchemexpress.cn/asperphenamate.html 研究领域：Autophagy | Metabolic Enzyme/Protease 作用靶点：Autophagy | Cathepsin 结构分类：其他类 In Vitro: Asperphenamate can inhibit cancer cell proliferation by fully inducing autophagy. asperphenamate showed inhibition effects against cathepsin L. At the same time, it also displayed weak inhibitory ability against cathepsin S. 相关产品：Natural Product Library Plus | Bioactive Compound Library Plus | Anti-Infection Compound Library | Immunology/Inflammation Compound Library | Metabolism/Protease Compound Library | Natural Product Library | Anti-Cancer Compound Library | Autophagy Compound Library | Microbial Metabolite Library | Angiogenesis-Related Compound Library | Anti-Cancer Natural Product Library | Protease Inhibitor Library | Membrane Protein-targeted Compound Library | Cell Death Library | Multi-Target Compound Library | Bioactive Compound Library Max | Leupeptin hemisulfate | N-Ethylmaleimide | Aloxistatin | PMSF | E-64 | Papain | CA-074 methyl ester | p-Aminophenylmercuric acetate | Calpeptin | CA-074 | L-Homocysteine | Z-FY-CHO | LY 3000328 | Odanacatib | SID 26681509 | Cathepsin inhibitor 1 | Z-FA-FMK | Balicatib | K777 | Chymostatin | S130 | Cathepsin L-IN-2 | Cathepsin G Inhibitor I | Cathepsin X-IN-1 | Petesicatib | Z-LVG-CHN2 | Cathepsin C-IN-5 | GSK-2793660 | L-006235 品牌介绍: MCE (MedChemExpress) 拥有数百种全球独家化合物，我们致力于为全球科研客户提供最新最全的高品质小分子活性化合物；10,000 多种高选择性抑制剂、激动剂涉及各热门信号通路及疾病领域；设有专业的实验中心和严格的质控、验证体系；提供 LC/MS、NMR、HPLC、手性分析、元素分析等各项质检报告，确保产品的高纯度、高品质；产品的生物活性多经各国客户实验验证；Nature, Cell, Science 等多种顶级期刊及制药专利收录了MCE客户的科研成果；专业团队跟踪最新的制药及生命科学研究进展，为您提供全球最新的活性化合物；与世界各大制药公司及知名科研机构建立了长期的合作。